A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561601



Internal ID334576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:182938952..182939605hg38UCSC Ensembl
chr4:183860105..183860758hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38654
hg19654
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16961246
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561601
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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